Ruiz Jonatan R, Fiuza-Luces Carmen, Buxens Amaya, Cano-Nieto Amalia, Gómez-Gallego Félix, Santiago Catalina, Rodríguez-Romo Gabriel, Garatachea Nuria, Lao José I, Morán María, Lucia Alejandro
Department of Physical Education and Sport, School of Physical Activity and Sport Sciences, University of Granada, Granada, Spain.
Age (Dordr). 2012 Oct;34(5):1269-83. doi: 10.1007/s11357-011-9296-3. Epub 2011 Sep 6.
Our study purpose was to compare a disease-related polygenic profile that combined a total of 62 genetic variants among (i) people reaching exceptional longevity, i.e., centenarians (n = 54, 100-108 years, 48 women) and (ii) ethnically matched healthy controls (n = 87, 19-43 years, 47 women). We computed a 'global' genotype score (GS) for 62 genetic variants (mutations/polymorphisms) related to cardiometabolic diseases, cancer or exceptional longevity, and also specific GS for main disease categories (cardiometabolic risk and cancer risk, including 36 and 24 genetic variations, respectively) and for exceptional longevity (7 genetic variants). The 'global' GS was similar among groups (centenarians: 31.0 ± 0.6; controls 32.0 ± 0.5, P = 0.263). We observed that the GS for hypertension, cancer (global risk), and other types of cancer was lower in the centenarians group compared with the control group (all P < 0.05), yet the difference became non significant after adjusting for sex. We observed significant between-group differences in the frequency of GSTT1 and GSTM1 (presence/absence) genotypes after adjusting for multiple comparisons. The likelihood of having the GSTT1 low-risk (functional) allele was higher in centenarians (odds ratio [OR] 5.005; 95% confidence interval [CI], 1.810-13.839), whereas the likelihood of having the GSTMI low-risk (functional) allele was similar in both groups (OR 1.295; 95% CI, 0.868 -1.931). In conclusion, we found preliminary evidence that Spanish centenarians have a lower genetic predisposition for cancer risk. The wild-type (i.e., functional) genotype of GSTT1, which is associated with lower cancer risk, might be associated with exceptional longevity, yet further studies with larger sample sizes must confirm these findings.
我们的研究目的是比较一种与疾病相关的多基因图谱,该图谱总共包含62个基因变异,涉及以下两组人群:(i)达到超长寿命的人群,即百岁老人(n = 54,年龄在100 - 108岁之间,48名女性);(ii)种族匹配的健康对照人群(n = 87,年龄在19 - 43岁之间,47名女性)。我们计算了与心脏代谢疾病、癌症或超长寿命相关的62个基因变异(突变/多态性)的“全局”基因型评分(GS),以及主要疾病类别(心脏代谢风险和癌症风险,分别包括36个和24个基因变异)和超长寿命(7个基因变异)的特定GS。两组之间的“全局”GS相似(百岁老人:31.0 ± 0.6;对照组32.0 ± 0.5,P = 0.263)。我们观察到,与对照组相比,百岁老人组中高血压、癌症(总体风险)和其他类型癌症的GS较低(所有P < 0.05),但在调整性别后差异变得不显著。在进行多重比较调整后,我们观察到GSTT1和GSTM1(存在/缺失)基因型频率在两组之间存在显著差异。百岁老人拥有GSTT1低风险(功能性)等位基因的可能性更高(优势比[OR] 5.005;95%置信区间[CI],1.810 - 13.839),而两组拥有GSTMI低风险(功能性)等位基因的可能性相似(OR 1.295;95% CI,0.868 - 1.931)。总之,我们发现初步证据表明西班牙百岁老人患癌症风险的遗传易感性较低。与较低癌症风险相关的GSTT1野生型(即功能性)基因型可能与超长寿命有关,但需要更大样本量的进一步研究来证实这些发现。